Canonical Allele Identifier: PA2825692551
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1038544
ClinVar RCV Id: RCV001341872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met182Thr
CA378920950
NM_001130442.3:c.545T>C